Whole exome sequencing frequently detects a monogenic cause in early onset nephrolithiasis and nephrocalcinosis

Ankana Daga, Amar J. Majmundar, Daniela A. Braun, Heon Yung Gee, Jennifer A. Lawson, Shirlee Shril, Tilman Jobst-Schwan, Asaf Vivante, David Schapiro, Weizhen Tan, Jillian K. Warejko, Eugen Widmeier, Caleb P. Nelson, Hanan M. Fathy, Zoran Gucev, Neveen A. Soliman, Seema Hashmi, Jan Halbritter, Margarita Halty, Jameela A. KariSherif El-Desoky, Michael A. Ferguson, Michael J.G. Somers, Avram Z. Traum, Deborah R. Stein, Ghaleb H. Daouk, Nancy M. Rodig, Avi Katz, Christian Hanna, Andrew L. Schwaderer, John A. Sayer, Ari J. Wassner, Shrikant Mane, Richard P. Lifton, Danko Milosevic, Velibor Tasic, Michelle A. Baum, Friedhelm Hildebrandt

Research output: Contribution to journalArticlepeer-review

98 Citations (Scopus)

Fingerprint

Dive into the research topics of 'Whole exome sequencing frequently detects a monogenic cause in early onset nephrolithiasis and nephrocalcinosis'. Together they form a unique fingerprint.

Medicine and Dentistry